TGFB1 missense variants in ExAC


The table below lists the TGFB1 missense variants found in the ExAC population database. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.




No. Genomic coord. Variant (CDS) Variant (Protein) Variant Type ExAC frequencyPopulations*
1. 41858921 c.29C>T p.P10L missense 0.56228983
2. 41858876 c.74G>C p.R25P missense 0.07922884
3. 41847860 c.788C>T p.T263I missense 0.02461013
4. 41858921 c.29C>G p.P10R missense 0.00064051
5. 41838037 c.1010G>C p.S337T missense 0.00063581
6. 41838160 c.887G>A p.R296Q missense 0.00038626
7. 41858864 c.86G>A p.G29E missense 0.00036210
8. 41854261 c.455G>A p.R152Q missense 0.00021418
9. 41858650 c.300G>T p.E100D missense 0.00017380
10. 41850733 c.553C>T p.R185W missense 0.00015778
11. 41858612 c.338T>C p.M113T missense 0.00014836
12. 41858939 c.11C>T p.S4F missense 0.00010404
13. 41858937 c.13G>C p.G5R missense 0.00010343
14. 41847926 c.722C>T p.T241I missense 0.00009128
15. 41854317 c.399G>A p.M133I missense 0.00008239
16. 41854262 c.454C>T p.R152W missense 0.00008238
17. 41854294 c.422G>A p.R141Q missense 0.00007414
18. 41858892 c.58G>C p.V20L missense 0.00007329
19. 41837091 c.1039A>T p.N347Y missense 0.00007159
20. 41858865 c.85G>A p.G29R missense 0.00006279
21. 41850673 c.613C>T p.R205W missense 0.00006066
22. 41858864 c.86G>C p.G29A missense 0.00006035
23. 41850657 c.629G>A p.R210H missense 0.00005942
24. 41837075 c.1055C>T p.A352V missense 0.00005758
25. 41858842 c.108C>G p.I36M missense 0.00005391
26. 41850682 c.604G>A p.G202R missense 0.00005280
27. 41848104 c.683G>A p.R228K missense 0.00005042
28. 41847933 c.715T>A p.F239I missense 0.00004981
29. 41858792 c.158T>C p.I53T missense 0.00004524
30. 41847857 c.791C>T p.P264L missense 0.00004142
31. 41837042 c.1088C>G p.P363R missense 0.00003841
32. 41848105 c.682A>G p.R228G missense 0.00003794
33. 41838175 c.872A>C p.K291T missense 0.00003417
34. 41854274 c.442G>A p.V148M missense 0.00003295
35. 41837016 c.1114C>T p.R372C missense 0.00003120
36. 41858744 c.206C>T p.P69L missense 0.00002916
37. 41850732 c.554G>A p.R185Q missense 0.00002745
38. 41838139 c.908G>A p.R303H missense 0.00002489
39. 41847884 c.764G>A p.R255Q missense 0.00002487
40. 41854264 c.452C>T p.S151F missense 0.00002471
41. 41858735 c.215C>A p.P72Q missense 0.00002433
42. 41850763 c.523A>G p.S175G missense 0.00002189
43. 41858694 c.256G>T p.D86Y missense 0.00002105
44. 41858684 c.266C>T p.A89V missense 0.00001965
45. 41850747 c.539G>A p.R180Q missense 0.00001739
46. 41838181 c.866C>T p.T289M missense 0.00001729
47. 41838140 c.907C>T p.R303C missense 0.00001660
48. 41847927 c.721A>G p.T241A missense 0.00001660
49. 41847867 c.781A>T p.M261L missense 0.00001657
50. 41838111 c.936C>G p.H312Q missense 0.00001653
51. 41850742 c.544C>T p.L182F missense 0.00001651
52. 41838046 c.1001C>T p.T334M missense 0.00001651
53. 41850742 c.544C>G p.L182V missense 0.00001651
54. 41838077 c.970G>A p.G324R missense 0.00001650
55. 41854310 c.406A>T p.N136Y missense 0.00001648
56. 41848126 c.661G>T p.A221S missense 0.00001439
57. 41850735 c.551A>G p.N184S missense 0.00001430
58. 41848101 c.686A>G p.D229G missense 0.00001245
59. 41848097 c.690C>G p.N230K missense 0.00001228
60. 41858702 c.248G>C p.S83T missense 0.00001114
61. 41858690 c.260G>C p.R87P missense 0.00001030
62. 41850698 c.588A>C p.L196F missense 0.00000932
63. 41858664 c.286G>A p.E96K missense 0.00000887
64. 41858658 c.292G>A p.E98K missense 0.00000879
65. 41850679 c.607G>A p.V203I missense 0.00000875
66. 41858655 c.295C>A p.P99T missense 0.00000873
67. 41858613 c.337A>G p.M113V missense 0.00000872
68. 41858644 c.306C>G p.D102E missense 0.00000866
69. 41850672 c.614G>A p.R205Q missense 0.00000865
70. 41850661 c.625A>C p.S209R missense 0.00000852
71. 41850658 c.628C>T p.R210C missense 0.00000849
72. 41847924 c.724G>A p.G242S missense 0.00000830
73. 41847930 c.718A>C p.T240P missense 0.00000830
74. 41847930 c.718A>G p.T240A missense 0.00000830
75. 41847885 c.763C>T p.R255W missense 0.00000829
76. 41847899 c.749T>G p.I250S missense 0.00000829
77. 41847900 c.748A>G p.I250V missense 0.00000829
78. 41847863 c.785C>T p.A262V missense 0.00000828
79. 41838125 c.922T>C p.W308R missense 0.00000827
80. 41847797 c.851A>G p.Y284C missense 0.00000827
81. 41847830 c.818G>A p.S273N missense 0.00000827
82. 41847809 c.839T>C p.L280P missense 0.00000827
83. 41847827 c.821C>T p.S274F missense 0.00000827
84. 41838037 c.1010G>A p.S337N missense 0.00000826
85. 41838094 c.953A>G p.H318R missense 0.00000826
86. 41838102 c.945G>C p.K315N missense 0.00000826
87. 41838103 c.944A>G p.K315R missense 0.00000826
88. 41838050 c.997G>A p.D333N missense 0.00000825
89. 41838074 c.973C>G p.P325A missense 0.00000825
90. 41838080 c.967C>T p.L323F missense 0.00000825
91. 41838055 c.992G>C p.S331T missense 0.00000825
92. 41838086 c.961T>C p.F321L missense 0.00000825
93. 41838056 c.991A>G p.S331G missense 0.00000825
94. 41854273 c.443T>C p.V148A missense 0.00000824
95. 41854211 c.505G>C p.E169Q missense 0.00000824
96. 41854274 c.442G>T p.V148L missense 0.00000824
97. 41854321 c.395A>G p.Y132C missense 0.00000824
98. 41854342 c.374A>G p.K125R missense 0.00000824
99. 41854261 c.455G>T p.R152L missense 0.00000824
100. 41854288 c.428C>T p.A143V missense 0.00000824
101. 41854347 c.369G>T p.K123N missense 0.00000824

* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish. Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.

Genomic coordinates refer to the GRCh37 release of the human genome.